Merck
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Regulatory Affairs Manager
Job Description PRIMARY ACTIVITIES 1. <Primary activities 1> • Prepare plan and set up process for filing new medicine applications and maintenance of registration of existing company's products with regulatory…
Specialist, Regulatory Affairs
Job Description At our company, we aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and…
R&D CMC Regulatory Affairs, Biologics CMC Sr. Scientist（CMC薬事）
Job Description グローバル研究開発本部 薬事領域スタッフとして、バイオ医薬品・ワクチンの新薬の開発開始から承認申請及び承認取得、並びに剤形追加及び変更管理に至るまでのCMC薬事業務に貢献していただける担当者を求めています。最先端のCMC技術を取り入れた製品開発や、製薬業界において注目されているCMC薬事関連トピックの協議に最前線で関与できる幅広い機会があります。…
R&D CMC Regulatory Affairs, Chemical Products Sr. Scientist（CMC薬事）
Job Description グローバル研究開発本部 薬事領域スタッフとして、化成品の新薬の開発開始から承認申請及び承認取得、並びに剤形追加及び変更管理に至るまでのCMC薬事業務に貢献していただける担当者を求めています。最先端のCMC技術を取り入れた製品開発や、製薬業界において注目されているCMC薬事関連トピックの協議に最前線で関与できる幅広い機会があります。…
Manager, Regulatory Affairs
Job Description Position Overview Independently manage projects of pipeline products and registered products, include but not limit to CTA, NDA, Renewal, Variations and related regulatory agency interactions. Achieve…
Senior Specialist Regulatory Affairs (Oncology)
Job Description We are looking for a Regulatory Affairs Manager (Senior Specialist) to join our Regulatory Team in Mexico. Position Overview The Regulatory Affairs Manager will be responsible for ensuring the timely…
Associate Director, Regulatory Affairs-CMC
Job Description Role Overview: The Associate Director of Regulatory Operations Content Management will serve as a strategic business partner and subject matter expert (SME) supporting the advancement of Regulatory…
Reporting and Solutions - Senior Specialist, Regulatory Affairs
Job Description Senior Specialist – Submission Planning & Requirements Management Role Overview The Submission Planning and Requirements Management (SPRM) team manages the submission planning capability for Global…
Associate Director, Regulatory Affairs
Job Description Job Description Reports to Regulatory Operations (RegOps) Director in OPAR. The RegOps Associate Director is responsible for the review, approval, and oversight of regulatory submissions to the…
Associate Specialist, Regulatory Affairs
Job Description Associate Specialist, Regulatory Affairs New MA applications for assigned products • Under supervision, performs timely and correct submissions and approvals of assigned new Marketing Authorization…
Regulatory Affairs Intern
Job Description Regulatory Affairs Intern opportunity is open UAE Nationals Duration: 4-8 Weeks Location: Dubai, United Arab Emirates Our company is committed to developing local talent and supporting the next…
Associate Director , Regulatory Affairs
Job Description Associate Director, Regulatory Affairs Registration of products for the Indian Market. To ensure compliance to all applicable laws and regulations in respect of Own and Contract Manufacturing of…
Regulatory Affairs Liaison (Associate Director)
Job Description The Regulatory Affairs Liaison (Associate Director) role is a broad role encompassing all aspects of regulatory strategy to support countries in region, including clinical, CMC and risk management…
Asso. Manager, Regulatory Affairs (Animal Health)
Job Description 职位名称 / Job Title 法规事务助理经理（Associate Manager, Regulatory Affairs） 岗位使命 / Mission 通过高质量、高效率的产品生命周期管理与合规运营，确保已上市兽用疫苗产品持续合规、稳定供应。 Ensure the ongoing compliance and reliable supply of marketed veterinary…
Intern- Regulatory Affairs- CMC
Job Description Our company starts your journey on the career path within the pharmaceutical industry. Not only will you learn skills both technical and professional but work on projects that will contribute towards…
Animal Health, Regulatory Affairs
Job Description POSITION OVERVIEW: The Associate Director of the Regulatory Affairs (RA) is responsible for the management of regulatory affairs activities including pharmacovigilance work at RA department at PDRA…